Form 483

Apex Medical Technologies, Inc. Form 483, 2011-11-30

FDA issued a Form 483 to Apex Medical Technologies, Inc. on 2011-11-30 with 4 public-safe observations.

483· Form 483 issued4 observations

Apex Medical Technologies, Inc. · San Diego, United States · Issued November 30, 2011

Overview

  • 4 public-safe observations are available for this inspection.
  • 4 structured CFR citations are represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

30 Nov 2011
21 CFR 820.20(c)

Management review - Lack of or inadequate procedures

Cited by Scott K Zika

30 Nov 2011
21 CFR 820.40(a)

Not approved or obsolete document retrieval

Cited by Scott K Zika

30 Nov 2011
21 CFR 820.70(f)

Buildings

Cited by Scott K Zika

30 Nov 2011
21 CFR 820.198(a)

Lack of or inadequate complaint procedures

Cited by Scott K Zika

Inspected site

AMApex Medical Technologies, Inc.San Diego, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 820.198(a)Cited across public-safe Form 483 observations1x
21 CFR 820.20(c)Cited across public-safe Form 483 observations1x
21 CFR 820.40(a)Cited across public-safe Form 483 observations1x
21 CFR 820.70(f)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 4 observations

Every observation in full, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere